Phan A, Touzet S, Dalle S, Ronger-Savlé S, Balme B, Thomas L
Department of Dermatology, Hôtel Dieu, Claude Bernard University, 69288 Lyon cedex 02, France.
Br J Dermatol. 2007 Aug;157(2):311-8. doi: 10.1111/j.1365-2133.2007.08031.x. Epub 2007 Jun 26.
Acral lentiginous melanoma (ALM) is the fourth histopathological subtype of malignant melanoma, accounting for < 10% of all melanomas in white-skinned populations. It is characterized by a lentiginous pattern of proliferation of the intraepidermal component of the tumour. Its individualization is still controversial, especially in regard of its prognostic value.
To characterize better ALM from a pathological point of view and to assess the prognostic value of all histopathological features of ALM.
We performed a review of all cases of ALM followed from 1996 to 2004 at the University Hospital Department of Dermatology, Lyon, France. We examined all haematoxylin, eosin and saffron-stained tissue sections of the primary lesions. Several pathological parameters of interest in melanoma were evaluated for disease-free and specific survival with the Kaplan-Meier method and the Cox proportional hazards regression model.
Representative histological material was available for 121 patients. The mean Breslow thickness was 2.5 mm (in situ-20 mm). Fifteen lesions (12%) were in situ, nine (7%) were at Clark level II, 35 (29%) at III, 40 (33%) IV and 22 (18%) V. Extension along adnexal structures was found in almost half of the ALMs (46%), without prognostic significance. Seventeen (14%) lesions showed no microscopic pigmentation. Remnants of pre-existing naevus were found in four (3%) melanomas. The width of the 36 (30%) ulcerated lesions ranged from 1 to 20 mm (mean 7.6). Ulceration and its width were both associated with a large tumour thickness (P < 0.01), a high level of invasion (P < 0.01), the presence of vascular invasion (P < 0.01) and the lack of pigment production (P < 0.01). Among the 99 ALMs which were in the vertical growth phase (VGP), 21 showed a high mitotic rate (> 6 mitoses mm(-2)). A high mitotic rate was found to be significantly associated with the presence of ulceration (P < 0.01). The presence of microscopic satellites was noted in 10 (10%) lesions. The uncommon presence of small cells (8%) in the VGP was statistically significantly (P < 0.01) associated with a worse prognosis compared with other cell types. Multivariate analysis identified mitotic rate (P < 0.01), microsatellites (P = 0.05), Clark level (P = 0.01) and gender (P = 0.03) as independent prognostic factors for disease-free survival. Only the presence of microsatellites (P = 0.02) and a high mitotic rate (P < 0.01) were independently correlated with specific survival in ALM.
This is a detailed pathological study of a large cohort with ALM, an uncommon subtype of melanoma. Mitotic activity appears to be of particular importance in predicting the outcome of ALM.
肢端雀斑样痣黑素瘤(ALM)是恶性黑素瘤的第四种组织病理学亚型,在白种人群中占所有黑素瘤的比例不到10%。其特征为肿瘤表皮内成分呈雀斑样增殖模式。其个体化仍存在争议,尤其是在预后价值方面。
从病理学角度更好地描述ALM,并评估ALM所有组织病理学特征的预后价值。
我们对1996年至2004年在法国里昂大学医院皮肤科随访的所有ALM病例进行了回顾。我们检查了所有原发性病变的苏木精、伊红和番红染色组织切片。使用Kaplan-Meier法和Cox比例风险回归模型评估黑素瘤中几个感兴趣的病理参数的无病生存期和特异性生存期。
有121例患者的代表性组织学材料。平均Breslow厚度为2.5mm(原位癌至20mm)。15个病变(12%)为原位癌,9个(7%)为Clark II级,35个(29%)为III级,40个(33%)为IV级,22个(18%)为V级。几乎一半的ALM(46%)发现有沿附属器结构的扩展,无预后意义。17个(14%)病变无显微镜下色素沉着。4例(3%)黑素瘤中发现有既往痣的残留。36个(30%)溃疡病变的宽度为1至20mm(平均7.6mm)。溃疡及其宽度均与肿瘤厚度大(P<0.01)、侵袭程度高(P<0.01)、血管侵袭的存在(P<0.01)和色素产生缺乏(P<0.01)相关。在99个处于垂直生长期(VGP)的ALM中,21个显示有高有丝分裂率(>6个有丝分裂/mm²)。发现高有丝分裂率与溃疡的存在显著相关(P<0.01)。10个(10%)病变中发现有显微镜下卫星灶。与其他细胞类型相比,VGP中少见的小细胞(8%)在统计学上与较差的预后显著相关(P<0.01)。多变量分析确定有丝分裂率(P<0.01)、卫星灶(P=0.05)、Clark分级(P=0.01)和性别(P=0.03)为无病生存期的独立预后因素。在ALM中,仅卫星灶的存在(P=0.02)和高有丝分裂率(P<0.01)与特异性生存期独立相关。
这是一项对大量ALM队列(黑素瘤的一种罕见亚型)的详细病理学研究。有丝分裂活性在预测ALM的预后方面似乎尤为重要。